Fig. 4.
Fig. 4. Localization of T and B cells homing into spleen. T and B cells were enriched from spleen of DDD/1-+/+, labeled with BCECF-AM (Dojindo), and 5 × 107 of the cells were intravenously injected into DDD/1-+/+ and DDD/1-plt/plt. Spleens from recipients were frozen at 48 hours after the injection. Cryostat section of the spleen was stained with MOMA-1 MoAb (BMA Biomedicals Ltd) and Cy5-conjugated antirat IgG (Amersham) to identify MZM, then examined under a confocal laser microscope system (Bio-Rad). The region sorrounded by MZM (red, indicated by arrowheads) is white pulp. Injected T or B cells (green) were identified in white pulp (thick arrow) and in red pulp (thin arrow). Bar at the lower right corner indicates 250 μm.

Localization of T and B cells homing into spleen. T and B cells were enriched from spleen of DDD/1-+/+, labeled with BCECF-AM (Dojindo), and 5 × 107 of the cells were intravenously injected into DDD/1-+/+ and DDD/1-plt/plt. Spleens from recipients were frozen at 48 hours after the injection. Cryostat section of the spleen was stained with MOMA-1 MoAb (BMA Biomedicals Ltd) and Cy5-conjugated antirat IgG (Amersham) to identify MZM, then examined under a confocal laser microscope system (Bio-Rad). The region sorrounded by MZM (red, indicated by arrowheads) is white pulp. Injected T or B cells (green) were identified in white pulp (thick arrow) and in red pulp (thin arrow). Bar at the lower right corner indicates 250 μm.

Close Modal

or Create an Account

Close Modal
Close Modal